@article {49851,
	title = {Ag(I)-catalyzed heterocyclization/[3+2] cycloaddition of α-alkynylenones with β-enaminones: tandem access to highly substituted cyclopenta[c]furans},
	journal = {Journal of Organic Chemistry},
	volume = {90},
	year = {2025},
	month = {SEP },
	pages = {12466-12479},
	type = {Article},
	abstract = {<p>
	A robust Ag(I)-catalyzed tandem heterocyclization/[3 + 2] cycloaddition of alpha-alkynylenones with beta-enaminones was developed, enabling efficient synthesis of cyclopenta[c]furans with good yields, operational simplicity, and broad substrate scope. In addition, it also presents an extended methodology to synthesize unsymmetrical tri(hetero)aryl methane having chromone and furan/pyrrole scaffolds by a slight modification of starting materials. Moreover, the synthesized cyclopenta[c]furans exhibit good fluorescence properties with quantum yields ranging from 0.33 to 0.53, as suggested by the photophysical studies.</p>
},
	issn = {0022-3263},
	doi = {10.1021/acs.joc.5c01707},
	author = {Vara, Vijay and Thete, Kishor R. and Panikar, Sera Deepu and Khan, Akram A. and Muthukrishnan, M.}
}
